CA2586011C - Tricyclic pyrazole derivatives as cannabinoid receptor modulators - Google Patents

Abstract

The present invention relates to novel compounds of general formula (I), their regioisomers, tautomeric forms, and novel intermediates involved in their synthesis.
The present invention also relates to a process of preparing compounds of general formula (I), their regioisomers, their tautomeric forms, their pharmaceutically acceptable salts, pharmaceutical compositions containing them, and novel intermediates involved in their synthesis. The compounds disclosed herein are useful as modulators of cannabinoid receptors.

Description

TRICYCLIC PYRAZOLE DERIVATIVES AS CANNABINOID RECEPTOR
MODULATORS
FIELD OF INVENTION

The present invention relates to novel compounds of general formula (I), their regioisomers, tautomeric forms, novel intermediates involved in their synthesis, their pharmaceutically acceptable salts and pharmaceutical compositions containing them.
The present invention also relates to a process of preparing compounds of general formula (I), their regioisomers, their tautomeric forms, their pharmaceutically acceptable salts, pharmaceutical compositions containing them, and novel intermediates involved in their synthesis.

X-(CH2)m N
(CH2)n' R3 /N
A N
Ar (~) BACKGROUND AND PRIOR ART
Cannabinoids are present in Indian hemp Cannabis sativa and have been well known for their medicinal properties for ages. Cannabinoids as a therapeutic agents is however a recent phenomenon. (Williamson E. M. & Evans E. J. Drugs 2000 Dec;
60(6): 1303-14) Research in this area over the last decade have provided very important information on the cannabinoid receptors and their agonists and antagonists.
Development of central Cannabinoid receptor ligands with lower lipophilicity.( J. Med.
Chem. 2003; 46:642-645) Further cloning and isolation of two different subtypes of cannabinoid receptors - CB1 (central subtype) and CB2 (peripheral subtype) and the first endogenous ligand N-arachidonyl ethanolamine amide(AEA); anadamide (Matsuda LA et. al., Nature 1990; 346:561-4; Devane WA et. al. J. Med. Chem.
1992;
35:2065-9; Munro, S. et. al., Nature 1993, 365, 61-5) have stimulated research in this field. There has also been an increased interest among the different pharmaceutical companies in developing drugs for the treatment of diseases connected with disorders of the cannabinoid systems (Greenberg D. A., Drugs News & Perspectives 1999;
12:
458; Kulkarni S. K. & Ninan, Indian Journal of Pharmacology 2001; 33: 170-184;
Piomelli D et, al., Trends Pharmacol Sci. 2000 Jun; 21(6): 218-24). Several compounds which are either CB, &/or CB2 antagonists have been reported and are under various stages of development for e.g. SR-141716 A(Sanofi), CP-27287 1(Pfizer), LY-(Eli Lily), AM-630 (Alexis), SR-144528(Sanofi) etc. Novel compounds which are selective CB I and/or CB2 antagonists, their preparation and their use in medicine have also been reported in US 5925768, US 6344474, US 6028084, US 5462960, EP
0656354, US 6432984, US 6509367 B1, US 5624941, EP1230222, EP 122952, FR
2816938, FR 2761266, FR 2800375, EP 0656354, EP 0576357, WO 03027076, WO
03026648, WO 03026647, WO 03020217, WO 0158450, WO 0185092, WO 0132663, WO 0132629.
Synthesis and biological evaluation of novel 4, 5-dihydro-lH-benzo [g]
indazole- based ligands for cannabinoid receptors has been described in Bioorg. Med Chem., 2005, 13, 3309-3320.
Synthesis of tricyclic pyrazole derivative (NESS 0327) as CB1 antagonist has been disclosed in J Pharmacology & Experimental Therapeutics, 2003, 306(1), 370. Synthesis and activity of tricyclic pyrazole ligands for CB 1 & CB2 receptors have been disclosed in Bioorg. Med. Chem., 2003, 11, 251-263.
Structure elucidation of novel ring constrained biaryl pyrazole CB 1 cannabinoid receptor antagonist has been described in Magn. Reson. Chem. 2003, 41, 265-268.
Synthesis and biological activity of rigid cannabinoid CB 1 cannabinoid receptor antagonists has been disclosed in Chem.Pharm.Bull.2002, 50, 1109-1113.
Tricyclic benzopyrazole derivatives as cyclooxygenase-2 (COX-2) inhibitors have been disclosed in WO 9609304.
Though research in the area of cannabinoids have been going on for more than a decade there are only few medicines available which modulate the cannabinoid receptors and fewer with minor side effects. Looking at the beneficial effects of cannabinoids, it would be highly desired to develop compounds, which modulate the cannabinoid receptors, having better or comparable absorption, metabolic stability, and exhibiting lesser toxicity.

SUMMARY OF INVENTION
In one exemplary embodiment there is provided compounds of general formula (I):

(CH\Rs r r 5 their tautomeric forms, their pharmaceutically acceptable salts, wherein `Ar' represents single or fused groups selected from aryl, optionally substituted with groups selected from halo or linear alkyl, and optionally substituted branched alkyl groups.
`A' represents a substituted aryl and X is selected from 0, S, SO, SO2 or NR', where R' represents H, or an optionally substituted group selected from linear alkyl, branched alkyl, and cycloalkyl groups, and m & n each represent an integer such that m is 1 or 2 and n is 1, 2 or 3; and wherein the substitution on A is selected from halogen, hydroxyl, and substituted groups selected from linear and branched alkyl groups. R1 represents 0 or S, R2 is either H or (C1-C6) alkyl; R3 is -NRbR,_, Rb & R,, each represents an optionally substituted group selected from alkyl, aralkyl and alkenyl, or Rb &
R, together with the nitrogen atom to which they are bonded, form a saturated or unsaturated heterocyclic or heteroaromatic radical.
In another exemplary embodiment there is provided an intermediate compound of the formula:

X-(CH2)m O
(CH2) , COOK
A O
(2) wherein `A' represents substituted aryl, X is selected from 0, S, SO, SO2, and NR', where R' represents H, or an optionally substituted group selected from a linear or branched alkyl, and cycloalkyl groups and m & n represents integers such that m is 1 or 2 and n is 1, 2 or 3; the substitution on A is selected from halogen, hydroxyl, and 2a substituted groups selected from linear and branched alkyl groups; R
represents an alkyl group which is a linear or branched radical containing one to eight carbons.
Certain other exemplary embodiments provide a pharmaceutical composition which comprises a compound of formula (I), as defined herein together with a pharmaceutically acceptable carrier, diluent or excipient.
The present invention describes novel compounds useful as modulators of cannabinoid receptors. The novel compounds are defined by the general formula (I) below:

2b X-'(CHz)m N R2 (CH2) / t R3 /N
A N

The compounds of the present invention mimic the actions of the cannabinoids making them useful for preventing or reversing the symptoms that can be treated with cannabis, some of its derivatives, and synthetic cannabinoids in a human or other mammalian subject. Preferably, the compounds of the present invention are selective antagonists of the cannabis CB1-receptor.
PREFERRED EMBODIMENTS OF THE INVENTION
The object of the present invention thus is to provide novel compounds of general formula (I), their tautomeric forms, their regioisomers, novel intermediates involved in their synthesis, their pharmaceutically acceptable salts and pharmaceutical compositions containing them or their mixtures and their use in medicine.

X-(CH2)m N
(CH2)n R3 /N
A N

In an embodiment of the present invention is provided a process for the' preparation of novel compounds of general formula (I), their regioisomers, their .
tautomeric forms, novel intermediates involved in their synthesis, pharmaceutically acceptable salts and pharmaceutical compositions containing them.
In another embodiment is provided pharmaceutical compositions containing compounds of general formula (I), their tautomeric forms, their regioisomers, their pharmaceutically acceptable salts and their mixtures having pharmaceutically acceptable carriers, solvents, diluents, excipients and other media normally employed in their manufacture.
In a further embodiment is provided a method of treatment of diseases which can be treated or whose symptoms can be reversed with cannabis or their derivatives both natural and synthetic, by administering a therapeutically effective & non-toxic amount of the compound of formula (I) or their pharmaceutically acceptable compositions to the mammals.

DETAILED DESCRIPTION
The novel compounds of the present invention are defined by the general formula (I) below:

X-(CH2)m (CH2)n R3 /N
A N

wherein `Ar' represents single or fused groups selected from aryl, aralkyl, heterocyclyl, heteroaryl, heterocyclyl(C1-C12)alkyl & heteroar(C1-C12)alkyl group, each of them independently may optionally be substituted;
`A' represents optionally substituted heteroaromatic groups, "X' is selected 1o from -CH2-, 0, S, SO, SO2, or NR', where R' represents H, optionally substituted groups selected from linear or branched alkyl and cycloalkyl groups and, m & n represents integers such that 1 <m+n<-3; or `A' represents substituted aromatic group, "X' may be selected from 0, S, SO, SO2, or NR', where R' represents H, optionally substituted groups selected from linear or branched alkyl, and cycloalkyl groups and m & n represents integers such that 2<-m+n<-3; or `A' represents optionally substituted heterocyclic groups, "X' may be selected from -CH2-, 0, S, SO, SO2, or NR', where R' represents H, optionally substituted groups selected from linear or branched alkyl and cycloalkyl groups and m & n represents integers such that 1 <_m+n:!3; or `A' represents optionally substituted alicyclic groups, "X' may be selected from -CH2-, 0, S, SO, SO2,. or NR', where R' represents H, optionally substituted groups selected from linear or branched alkyl and cycloalkyl groups and m & n represents integers such that 1 <-m+n<-3; or R1 represents 0, S, or the group represented by N-Q, where Q represents H, substituted or unsubstituted groups selected from alkyl, aralkyl, aryl, heteroaryl or heterocyclic groups or the group represented by SO2R", where R" represents H, -OH, halogen or substituted or unsubstituted groups selected from alkyl, aralkyl, aryl, heteroaryl or heterocyclic or alicyclic groups;

R2 is either H or (C1-C6) alkyl; R3 is -NRaRbRc or NRbRC where Ra is (C1-C6)alkyl or Ra forms a bridge, containing 1-2 atoms, with one of the atoms of the heterocyclic radical formed by -NRbRc;
Rb and Rb represents optionally substituted groups selected from alkyl, aralkyl or alkenyl or Rb & Rb together with the nitrogen atom to which they are bonded, form a saturated or unsaturated heterocyclic or heteroaromatic radical which may be optionally substituted and may be fused;
The substituents on `A' may be selected from hydroxyl, oxo, halo, thio, nitro, amino, cyano, formyl, optionally substituted groups selected from linear or branched alkyl, haloalkyl, perhaloalkyl, alkoxy, haloalkoxy, perhaloalkoxy, alkenyl, alkynyl, alkoxy, alkenoxy, acyl, acyloxy, acylamino, monosubstituted or disubstituted amino, carboxylic acid and its derivatives such as esters and amides, carbonylamino, hydroxyalkyl, aminoalkyl, alkoxyalkyl, alkylthio, thioalkyl, alkoxycarbonylamino, aminocarbonylamino, alkylaminocarbonylamino, alkoxyamino, hydroxyl amino groups; preferably, the substituents on `A' may be selected from halogen, hydroxyl, thio, nitro, amino, cyano, optionally substituted groups selected from linear or branched alkyl, alkoxy, thioalkyl, haloalkyl, haloalkoxy, acyl, aminoalkyl groups;
The substituents on `Ar' may be selected from hydroxy, halo, thio, nitro, amino, cyano, formyl, or optionally substituted groups selected from amidino, linear or branched alkyl, haloalkyl, perhaloalkyl, alkoxy, haloalkoxy, perhaloalkoxy, alkenyl, alkynyl, alkoxy, alkenoxy, monosubstituted or disubstituted amino, carboxylic acid and its derivatives such as esters and amides, carbonylamino, hydroxyalkyl, aminoalkyl, alkoxyalkyl, alkylthio, thioalkyl, alkylsulfonylamino, alkylsulfonyloxy, alkoxycarbonylamino, hydroxyl amino, sulfenyl derivatives, sulfonyl derivatives, sulfonic acid and its derivatives; preferably the substituents on `Ar' may be selected from hydroxy, halo, amino or optionally substituted groups selected from linear or branched alkyl, monosubstituted or disubstituted amino, alkoxy, acyl, alkylthio, arylthio, alkylsulfonylamino, alkylsulfonyloxy, carboxylic acid and its derivatives such as esters and amides;
The substituents on `A', or `Ar' may further be optionally substituted by any of the groups as mentioned above.
In a preferred embodiment the groups, radicals described above may be selected from:

- the "alkyl" group used either alone or in combination with other radicals, denotes a linear or branched radical containing one to eight carbons, selected from methyl, ethyl, n-propyl, iso-propyl, n-butyl, sec-butyl, tert-butyl, amyl, t-amyl, n-pentyl, n-hexyl, iso-hexyl, heptyl, octyl and the like;
- the "alkenyl" group used either alone or in combination with other radicals, is selected from a radical containing from two to twelve carbons, more preferably groups selected from vinyl, allyl, 2-butenyl, 3-butenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, 2-hexenyl, 3-hexenyl, 4-hexenyl, 5-hexenyl, 2-heptenyl, 3-heptenyl, heptenyl, 5-heptenyl, 6-heptenyl and the like; the "alkenyl" group includes dienes and trienes of straight and branched chains;
- the "alkynyl" group used either alone or in combination with other radicals, is selected from a linear or branched radical containing two to twelve carbon atoms, more preferably thynyl, 1-propynyl, 2-propynyl, 1-butynyl, 2-butynyl, 3-butynyl, 1-pentynyl, 2-pentynyl, 3-pentynyl, 4-pentynyl, 1-hexynyl, 3-hexynyl, 4-hexynyl, hexynyl, and the like. The term "alkynyl" includes di- and tri-ynes;
- the "cycloalkyl" or "alicyclic" group used either alone or in combination with other radicals, is selected from a cyclic radical containing three to seven carbons, more preferably cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and the like;

- the "cycloalkenyl" group used either alone or in combination with other radicals, are preferably selected from cyclopropenyl, 1-cyclobutenyl, 2-cylobutenyl, 1-cyclopentenyl, 2-cyclopentenyl, 3-cyclopentenyl, 1-cyclohexenyl, 2-cyclohexenyl, 3-cyclohexenyl, 1-cycloheptenyl, cycloheptadienyl, cycloheptatrienyl, and the like;
- the "alkoxy" group used either alone or in combination with other radicals, is selected from groups containing an alkyl radical, as defined above, attached directly to an oxygen atom, ' more preferably groups selected from methoxy, ethoxy, n-propoxy, iso-propoxy, n-butoxy, t-butoxy, iso-butoxy, pentyloxy, hexyloxy, and the like;

- the "alkenoxy" group used either alone or in combination with other radicals, is selected from groups containing an alkenyl radical, as defined above, attached to an oxygen atom, more preferably selsected from vinyloxy, allyloxy, butenoxy, pentenoxy, hexenoxy, and the like;

- the "haloalkyl" group is selected from an alkyl radical, as defined above, suitably substituted with one or more halogens; such as perhaloalkyl, more preferably, perfluoro(Ci-C6)alkyl such as fluoromethyl, difluoromethyl,, trifluoromethyl, fluoroethyl, difluoroethyl, trifluoroethyl, mono or polyhalo substituted methyl, ethyl, propyl, butyl, pentyl or hexyl groups;
- the "haloalkoxy" group is selected from suitable haloalkyl, as defined above, directly attached to an oxygen atom, more preferably groups selected from fluoromethoxy, chloromethoxy, fluoroethoxy chloroethoxy and the like;
- the "perhaloalkoxy" group is selected from a suitable perhaloalkyl radical, as defined above, directly attached to an oxygen atom, more preferably groups selected from trifluoromethoxy, trifluoroethoxy, and the like;
- the "aryl" or "aromatic" group used either alone or in ' combination with other radicals, is selected from a suitable aromatic system containing one, two or three rings wherein such rings may be attached together in a pendant manner or may be fused, more preferably the groups are selected from phenyl, naphthyl, tetrahydronaphthyl, indane, biphenyl, and the like;
- the "heterocyclyl" or "heterocyclic" group used either alone or in combination with other radicals, is selected from suitable saturated, partially saturated or unsaturated aromatic or non aromatic mono, bi or tricyclic radicals, containing one or more heteroatoms selected from nitrogen, sulfur and oxygen, more preferably selected from aziridinyl, azetidinyl, pyrrolidinyl, imidazolidinyl, piperidinyl, piperazinyl, 2-oxopiperidinyl, 4-oxopiperidinyl, 2-oxopiperazinyl, 3-oxopiperazinyl, morpholinyl, thiomorpholinyl, 2-oxomorpholinyl, azepinyl, diazepinyl, oxapinyl, thiazepinyl, oxazolidinyl, thiazolidinyl, dihydrothiophene, dihydropyran, dihydrofuran, dihydrothiazole, benzopyranyl, benzopyranonyl, benzodihydrofuranyl, benzodihydrothienyl, pyrazolopyrimidonyl, azaquinazolinoyl, thienopyrimidonyl, quinazolonyl, ' pyrimidonyl, benzoxazinyl, benzoxazinonyl, benzothiazinyl, benzothiazinonyl, thieno piperidinyl, and the like; -- the "heteroaryl" or "heteroaromatic" group used either alone or in combination with other radicals, is selected from suitable single or fused mono, bi or tricyclic aromatic heterocyclic radicals containing one or more hetero atoms selected from 0, N or S, more preferably the groups are selected from pyridyl, thienyl, furyl, pyrrolyl, oxazolyl, thiazolyl, isothiazolyl, imidazolyl, isoxazolyl, oxadiazolyl, thiadiazolyl, triazolyl, tetrazolyl, benzopuranyl, benzothienyl, indolinyl, indolyl, azaindolyl, azaindolinyl, pyrazolopyrimidinyl, azaquinazolinyl, pyridofuranyl, pyridothienyl, thienopyrimidyl, quinolinyl, pyrimidinyl, pyrazolyl, quinazolinyl, pyridazinyl, triazinyl, benzimidazolyl, benzotriazolyl, phthalazynil, naphthylidinyl, purinyl, carbazolyl, phenothiazinyl, phenoxazinyl, benzoxazolyl, benzothiazolyl and the like;
- the "the groups "heteroaryloxy", "heteroaralkoxy", "heterocycloxy", "heterocylylalkoxy" are selected from suitable heteroaryl, heteroarylalkyl, heterocyclyl, heterocylylalkyl groups respectively, as defined above, attached to an oxygen atom;
- the "acyl" group used either alone or in combination with other radicals, is selected from a radical containing one to eight carbons, more preferably selected from formyl, acetyl, propanoyl, butanoyl, iso-butanoyl, pentanoyl, hexanoyl, heptanoyl, benzoyl and the like, which may be substituted;
- the "acyloxy" group used either alone or in combination with other radicals, is selected from a suitable acyl group, as defined above, directly attached to an oxygen atom, more preferably such groups are selected from acetyloxy, propionyloxy, butanoyloxy, iso-butanoyloxy, benzoyloxy and the like;
- the "acylamino" group used either alone or in combination with other radicals, is selected from a suitable acyl group as defined earlier, attached to an amino radical, more preferably such groups are selected from CH3CONH, C2H5CONH, C3H7CONH, C4H9CONH, C6H5CONH and the like, which may be substituted;
20. - the "mono-substituted amino" group used either alone or in combination with other radicals, represents an amino group substituted with one group selected from (C1-C6)alkyl, substituted alkyl, aryl, substituted aryl or arylalkyl groups as defined earlier, more preferably such groups are selected from methylamine, ethylamine, n-propylamine, n-butylamine, n-pentylamine and the like;
- the `disubstituted amino" group used either alone or in combination with other radicals, represents an amino group, substituted with two radicals that may be same or different selected from (C1-C6)alkyl, substituted alkyl, aryl, substituted aryl, or arylalkyl groups, as defined above, more preferably the groups are selected from dimethylamino, methylethylamino, diethylamino, phenylmethyl amino and the like;
- the "arylamino" used either alone or in combination with other radicals, represents an aryl group, as defined above, linked through amino having a free valence bond from the nitrogen atom, more preferably the groups are selected from phenylamino, naphthylamino, N-methyl anilino and the like;

the "oxo" or "carbonyl" group used either alone (-C=O-) or in combination with other radicals such as alkyl described above, for e.g. "alkylcarbonyl", denotes a carbonyl radical (-C=O-) substituted with an alkyl radical described above such as acyl or alkanoyl;
- the "carboxylic acid" group, used alone or in combination with other radicals, denotes a -COOH group, and includes derivatives of carboxylic acid such as esters and amides;

- the "ester" group used alone or in- combination with other radicals, denotes -COO-group, and includes carboxylic acid derivatives, more preferably the ester moieties are selected from alkoxycarbonyl, such as methoxycarbonyl, ethoxycarbonyl, and the like, which may optionally ' be substituted; aryloxycarbonyl group such as phenoxycarbonyl, napthyloxycarbonyl, and the like, which may optionally be substituted; aralkoxycarbonyl group such as benzyloxycarbonyl, phenethyloxycarbonyl, napthylmethoxycarbonyl, and the like, which may optionally be substituted; heteroaryloxycarbonyl, heteroaralkoxycarbonyl, wherein the heteroaryl group, is as defined above, which may optionally be substituted;
heterocyclyloxycarbonyl, where the heterocyclic group, as defined earlier, which may optionally be substituted;

- the "amide" group used alone or in combination with other radicals, represents an aminocarbonyl radical (H2N-C=O-), wherein the amino group is mono- or di-substituted or unsubstituted, more preferably the groups are selected from methylamide, dimethylamide, ethylamide, diethylamide, and the like;
- the "aminocarbonyl" group used either alone or in combination with other radicals, may be selected from `aminocarbonyl', `aminocarbonylalkyl", "n-alkylaminocarbonyl", "N-arylaminocarbonyl", "N,N-dialkylaminocarbonyl", "N-alkyl-N-arylaminocarbonyl", "N-alkyl-N-hydroxyaminocarbonyl", and "N-alkyl-N-hydroxyaminocarbonylalkyl", each of.them being optionally substituted. The terms "N-alkylaminocabonyl" and "N,N-dialkylaminocarbonyl" denotes aminocarbonyl radicals, as defined above, which have been substituted with one alkyl radical and with two alkyl radicals, respectively. Preferred are "lower alkylaminocarbonyl" having lower alkyl radicals as described above attached to aminocarbonyl radical. The terms "N-arylaminocarbonyl" and "N-alkyl-N-arylaminocarbonyl" denote amiocarbonyl radicals substituted, respectively, with one aryl radical, or one alkyl, and one aryl radical. The term "aminocarbonylalkyl"
includes alkyl radicals substituted with aminocarbonyl radicals;
- the "hydroxyalkyl" group used either alone or in combination with other radicals, is selected from an alkyl group, as defined above, substituted with one or more hydroxy radicals, more preferably the groups are selected from hydroxymethyl, hydroxyethyl, hydroxypropyl, hydroxybutyl, hydroxypentyl, hydroxyhexyl and the like;
- the "aminoalkyl" group used alone or in combination with other radicals, denotes an amino (-NH2) moiety attached to an alkyl radical, as defined above, which may be substituted, such as mono- and di-substituted aminoalkyl. The term "alkylamino"
used herein, alone or in combination with other radicals, denotes an alkyl radical, as defined above, attached to an amino group, which may be substituted, such as mono- and di-substituted alkylamino;
- the "alkoxyalkyl" group used alone or in combination with other radicals, denotes an alkoxy group, as defined above, attached to an alkyl group as defined above, more preferably the groups may be selected from methoxymethyl, ethoxymethyl, methoxyethyl, ethoxyethyl and the like;
- the "alkylthio" group used either alone or in combination with other radicals, denotes a straight or branched or cyclic monovalent substituent comprising an alkyl group as defined above, linked through a divalent sulfur atom having a free valence bond from the sulfur atom, more preferably the groups may be selected from methylthio, ethylthio, propylthio, butylthio, pentylthio and the like or cyclic alkylthio selected from cyclopropylthio, cyclobutylthio, cyclopentylthio, cyclohexylthio and the like, which may be optionally substituted;
- the "thioalkyl" group used either alone or in combination with other radicals, denotes an alkyl group, as defined above, attached to a group of formula -SR', where R' represents hydrogen, alkyl or aryl group, e.g. thiomethyl, methylthiomethyl, phenylthiomethyl and the like, which may be optionally substituted.
- the "alkoxycarbonylamino" group used alone or in combination with other radicals, is selected.from a suitable alkoxycarbonyl group, as defined above, attached to an amino group, more preferably methoxycarbonylamino, ethoxycarbonylamino, and the like;

- the "aminocarbonylamino", "alkylaminocarbonylamino", "dialkylaminocarbonylamino" groups used alone or in combination with other radicals, is a carbonylamino (-CONH2) group, attached to amino(NH2), alkylamino group or dialkylamino group respectively, where alkyl group is as defined above;
- the "amidino" group used either alone or in combination with other radicals, represents a -C(=NH)-NH2 radical; the "alkylamidino" group represents an alkyl radical, as described above, attached to an amidino group;
- the "hydrazino" group used either alone or in combination with other radicals, represents a group of the formula -NHNH-, suitably substituted with other radicals, selected from those described above such as an alkyl hydrazino, where an alkyl group, as defined above is attached to a hydrazino group;
- the "alkoxyamino" group used either alone or in combination with other radicals, represents a suitable alkoxy group as defined above, attached to an amino group;
- the "hydroxyamino" group used either alone or in combination with other radicals, represents a -NHOH moiety, and may be optionally substituted with suitable groups selected from those described above;
- the "sulfenyl" group or "sulfenyl derivatives" used alone or in combination with other radicals, represents a bivalent group, -SO- or RXSO, where R. is an optionally substituted alkyl, aryl, heteToaryl, heterocyclyl, group selected from those described above;
- the "sulfonyl" group or "sulfones derivatives" used either alone or in combination with other radicals, with other terms such as alkylsulfonyl, represents a divalent radical -SO2-, or RXSO2-, where R. is as defined above. More preferably, the groups may be selected from "alkylsulfonyl" wherein suitable alkyl radicals, selected from those defined above, is attached to a sulfonyl radical, such as methylsulfonyl, ethylsulfonyl, propylsulfonyl and the like, "arylsulfonyl"
wherein an aryl radical, as defined above, is attached to a sulfonyl radical, such as phenylsulfonyl and the like.
Suitable groups and substituents on the groups may be selected from those described anywhere in the specification.
Particularly useful compounds of the present invention are:
4-Chloro-N-{[8-chloro-l- (2, 4-dichloro-phenyl)-1, 4, 5, 6-tetrahydro-1, 2-diaza-benzo [e] azulene-3-yl]-methylamino-methylene}-benzenesulfonamide and its pharmaceutically acceptable salts;

8-chloro-l-(2, 4-dichloro-phenyl)-4, 5-dihydro-1H-6-oxa-1, 2-diaza-benzo [e]
azulene-3-carboxylic acid piperidin-1-ylamide and its pharmaceutically acceptable salts;
8-chloro-l-(2, 4-dichloro-phenyl)-4, 5-dihydro-1H-6-oxa-1, 2-diaza-benzo [e]
azulene-3-carboxylic acid -(4-hydroxy-piperidin-1-yl' -amide and its pharmaceutically acceptable salts;
8-chloro-l-(2, 4-dichloro-phenyl)-4, 5-dihydro-1H-6-oxa-1, 2-diaza-benzo [e]
azulene-3-carboxylic acid pyrrolidin-1-yl amide and its pharmaceutically acceptable salts;
8-chloro-l-(2, 4-dichloro-phenyl)-4, 5-dihydro-1H-6-oxa-1, 2-diaza-benzo [e]
azulene-3-carboxylic acid (hexahydro-cyclopenta[c] pyrrol-2-yl)-amide and its pharmaceutically acceptable salts;
8-chloro-l-(2, 4-dichloro-phenyl)-4, 5-dihydro-1H-6-oxa-1, 2-diaza-benzo [e]
azulene-3-carboxylic acid morpholine-4-yl-amide and its pharmaceutically acceptable salts;
8-chloro-l-(2, 4-dichloro-phenyl)-4, 5-dihydro-1H-6-oxa-1, 2-diaza-benzo [e]
azulene-3-carboxylic acid (4-methyl-piperazine-1-yl)-amide and its pharmaceutically acceptable salts;
8-chloro-l-(4-chloro-phenyl)-4, 5-dihydro-1H-6-oxa-1, 2-diaza-benzo [e]
azulene-3-carboxylic acid piperidin-1-ylamide and its pharmaceutically acceptable salts;
8-chloro-l-(4-chloro-phenyl)-4, 5-dihydro-1H-6-oxa-1, 2-diaza-benzo [e]
azulene-3-carboxylic acid pyrrolidin-1-ylamide and its pharmaceutically acceptable salts;
8-chloro-l-(4-chloro-phenyl)-4, 5-dihydro-1H-6-oxa-1, 2-diaza-benzo [e]
azulene-3-carboxylic acid morpholin-4-ylamide and its pharmaceutically acceptable salts;
8-chloro-l-(4-chloro-phenyl)-4, 5-dihydro-1H-6-oxa-1, 2-diaza-benzo [e]
azulene-3-carboxylic acid N'-cyclopropyl-hydrazide and its pharmaceutically acceptable salts;
8-chloro-l-(4-chloro-phenyl)-4, 5-dihydro-1H-6-oxa-1, 2-diaza-benzo [e]
azulene-3-carboxylic acid piperidin-1-ylamide and its pharmaceutically acceptable salts;

1-(2, 4-Dichloro-phenyl)-8-methyl-4, 5-dihydro-lH-6-oxa-1, 2-diaza-benzo [e]
azulene-3-carboxylic acid piperidin-1-ylamide and its pharmaceutically acceptable salts;
1-(2, 4-Dichloro-phenyl)-8-methyl-4, 5-dihydro-1H-6-oxa-1, 2-diaza-benzo [e]
azulene-3-carboxylic acid pyrrolidin-1-ylamide and its pharmaceutically acceptable salts;

1-(4-chloro-phenyl)-8-methyl-4, 5-dihydro-1H-6-oxa-1, 2-diaza-benzo [e]
azulene-3-carboxylic acid piperidin-l-ylamide and its pharmaceutically acceptable salts;
1-{[8-chloro-l-(2, 4-dichloro-phenyl)-1, 4, 5, 6 -tetrahydro-7-thia-1, 2-diaza-cyclopenta [e] azulene-3-carboxylic acid piperidin-1-ylamide and its pharmaceutically acceptable salts;
8-Chloro-l-(2, 4-dichloro-phenyl)-1, 4, 5, 6-tetrahydro-7-thia-1, 2-diaza-cyclopenta [e] azulene-3-carboxylic acid (hexahydro-cyclopenta [c] pyrrol-2-yl)-amide and its pharmaceutically acceptable salts;
8-Chloro-l-(2, 4-dichloro-phenyl)-4, 5-dihydro-1H-6, 7-dithia-1, 2-diaza-cyclopenta[e] azulene-3-carboxylic acid piperidin-1-ylamide and its pharmaceutically acceptable salts;

7-Chloro-l-(2, 4-dichloro-phenyl)-1, 5-dihydro-4, 6-dithia-1, 2-diaza-as-indacene-3-carboxylic acid piperidin-1-ylamide and its pharmaceutically acceptable salts;
7-Chloro-l-(2, 4-dichloro-phenyl)-1, 5-dihydro-4, 6-dithia-1, 2-diaza-as-indacene-3-carboxylic acid (hexahydro-cyclopenta [c] pyrrol-2-yl)-amide and its pharmaceutically acceptable salts;
8-Chloro-l-(2, 4-dichloro-phenyl)-4, 5-dihydro-1H-6-thia-1, 2-diaza-benzo [e]
azulene-3-carboxylic acid piperidin-l-ylamide and its pharmaceutically acceptable salts;
8-Bromo-l-(2, 4-dichloro-phenyl)-4, 5-dihydro-1H-6-oxa-1, 2-diaza-benzo [e]
azulene-3-carboxylic acid piperidin-l-ylamide and its pharmaceutically acceptable salts;

The compounds of the present invention may be prepared using the methods described below, together with conventional techniques known to those skilled in the art of organic synthesis, or variations thereon as appreciated by those skilled in the art.

Referred methods include, but are not limited to those described below, where all symbols are as defined earlier.
Scheme:
Compound of formula 2 by suitable modification of similar processes described earlier in the art [Chem. Pharm. Bull. 2002, 50, 1109-1113]. Compound of formula 4 may be prepared by refluxing 2 with suitable substituted hydrazine hydrochloride of formula 3, where `Ar' is as defined earlier, in suitable solvents such as MeOH, EtOH, propanol, isopropanol, butanol, t-butanol, acetic acid and the like or mixtures thereof.
Alkaline hydrolysis of 4 using suitable bases like NaOH, KOH, LiOH, AgNO3i Na2CO3, CsCO3 and the like in solvents such as methanol, methanol/water, methanol/THF or THF/H20 and the like or mixtures thereof gives the corresponding acid of formula 5. Compounds of formula 5 is first converted to their corresponding acid chloride by treating with suitable halogenating agents selected from SOC12, COC12, PC13, PC15 and the like in suitable solvents such toluene, benzene, xylene, dichloromethane, chloroform and the like or mixtures thereof. The acid chlorides generated in situ may be subsequently treated with suitable substituted or unsubstituted amines, bicyclic amines, substituted or unsubstituted hydrazines, to obtain compounds of formula (I).
The compound of formula 5 may optionally, after conversion to its corresponding acid chloride be treated with suitable compounds of formula 6, where `Q' is as defined earlier, in solvents selected from triethyl amine, DMSO, DMF, diisopropyl ethyl amine and the like or mixtures thereof to obtain the compounds of formula 7.
The compound of formula 7 on treatment with suitable halogenating agent such as SOC12, COC12, PC13, PC15 and the like in suitable solvents such toluene, benzene, xylene, dichloromethane, chloroform and the like or mixtures thereof to provide compounds of formula 8. The compound of formula 8 is stirred with suitable amines of formula NHR2R3, where R2 & R3 are as defined earlier, in solvents selected from methanol, ethanol, water, THE and the like to obtain compounds of formula (I).

Scheme :

X-(CH2)m 0 R
(C/ O o CIH3N.N.H (CH d COOR (3) Ar A O (2) Ar O X-(CH2)m H
X-(CH~m R2 1. SOC12tsolvent (C
(CH, n / N\ N~R3 2. NH /NON
~N q 1 A II) (5) Ar 1. SOC12lsolvent 2. NH2Q
(6) CI O
X--(CH2)m /Q X-(CH2)m NQ
(cH2) N (cam H
A N =--_.. A Ni solvent NHR2R3.
(9) N
X-(CH2),n N R2 N
(C \R3 \
A

The compounds of formula (I) may be optionally converted to their suitable pharmaceutically acceptable salts by suitable modifications of techniques and processes known to persons skilled in the art.
It will -be appreciated that in any of the above mentioned reactions any reactive group in the substrate molecule may be protected, according to conventional chemical practice. Suitable protecting groups in any of the above mentioned reactions are those used conventionally in the art. The methods of formation and removal of such protecting groups are those conventional methods appropriate to the molecule being protected. T. W. Greene and P. G. M. Wuts "Protective groups in Organic Synthesis", John Wiley & Sons, Inc, 1999, 3rd Ed., 201-245 along with references therein gives such conventional methods.

The novel compounds of the present invention can be formulated into suitable pharmaceutically acceptable compositions by combining with suitable excipients as are well known.

The compounds of Formula (I) or pharmaceutical compositions containing them may be administered either by oral, topical or parenteral administration.
The pharmaceutical composition is provided by employing conventional techniques. Preferably the composition is in unit dosage form containing an effective amount of the active component, that is, the compounds of formula (I) according to this invention.

The quantity of active component, that is, the compounds of formula (I) according to this invention, in the pharmaceutical composition and unit dosage form thereof may be varied or adjusted widely depending upon the particular application method, the potency of the particular compound and the desired concentration.
Generally, the quantity of active component will range between 0.5 % to 90 %
by weight of the composition.

The invention is explained in greater detail by the examples given below, which are provided by way of illustration only and therefore should not be construed to limit the scope of the invention.

It will be appreciated that one or more of the processes described in the general schemes above may be used to prepare the compounds of the present invention.
1H AMR spectral data given in the tables (vide infra) are recorded using a 300 MHz spectrometer (Bruker AVANCE-300) and reported in 8 scale. Until and otherwise mentioned the solvent used for NMR is CDC13 using tetramethyl silane as the internal standard.
Example 1 4-Chloro-N- {[8-chloro-1 (2 4-dichloro-phenyl,')-l, 4, 5, 6-tetrahydro-1, 2-diaza-benzo [el azulene-3-yl]-methylamino-meth ly ene}-benzenesulfonamide 8-chloro-l-(2, 4-dichloro-phenyl)-1, 4, 5, 6-tetrahydro-1, 2-diaza-benzo [e]
azulene-3-carboxylic acid was prepared by by suitable modifications of similar techniques and processes known in the art.
.Step A:

4-Chloro-N {8-chloro-l- (2, 4-dichloro-phenyl)-1, 4, 5, 6-tetrahydro-1, 2-diaza-benzo [e] azulene-3-carbonyl)-benzene-sulfonamide 8-Chloro-l-(2, 4-dichloro-phenyl)-1, 4, 5, 6-tetrahydro-1, 2-diaza-benzo [e]
azulene-3-carboxylic acid (4.3 g, 10.55 mmol) was converted into acid chloride using thionyl chloride (2.31 mL, 31.66 mmol) in toluene by refluxing at ca. 110 C over a period of 1 h.

The solvents were evaporated under reduced pressure. The residue obtained was taken in dichloromethane (20 mL) and the resulting solution was added to the cooled suspension of 4-chloro benzene sulfonamide (2.7 g, 4.137 mmol) and TEA (1.97 mL, 14.137 mmol) in dichloromethane (50 mL). The reaction mixture was stirred at ca. 27 C over a period of 30 min and diluted with water .(150 mL), extracted with dichloromethane.

The organic layer was separated, dried over anhydrous Na2SO4 and evaporated under reduced pressure to afford crude colorless oil. The oil was purified through column chromatography to afford 4-Chloro-N-{8-chloro-l- (2, 4-dichloro-phenyl)-1, 4, 5, 6-tetrahydro-1, 2-diaza-benzo [e] azulene-3-carbonyl)-benzene-sulfonamide (4.75 g, 8.175 mmol) as off white solid.

'HNMR (CDC13, 300 MHz): 6 9.38(s, 1H), 8.0(d, J= 8.4 Hz, 2H), 7.5(d, J= 8.4 Hz, 2H), 7.4(m, 3H), 7.2(dd, J= 9.9, 8.4 Hz, 1H), 6.9(dd, J= 6.3, 1.9 Hz, 1H), 6.5(d, J= 8.4 Hz, 1H), 2.6(t, J= 6.6, 6.3 Hz, 21-1), 2.2(br, 2H) 1.26(br, 2H).

Step B:

4-Chloro-N-{[8-chloro-l- (2, 4-dichloro-phenyl)-1, 4, 5, 6-tetrahydro-1, 2-diaza-benzo [e] azulene-3-yl]-methylamino-methylene}-benzenesulfonamide (Compound 1) 4-Chloro-N-{8-chloro-l-(2, 4-dichloro-phenyl)-1, 4, 5, 6-tetrahydro-1, 2-diaza-benzo [e] azulene-3-carbonyl)-benzene-sulfonamide (2.0 g, 3.44 mmol) and PCl5 (1.56 g, 6.88 mmol) in chlorobenzene (20 mL) were refluxed at ca. 120 C over a period of 3.0 h. The solvents were evaporated under reduced pressure to afford yellow gummy solid.
The gummy solid was taken in dichloromethane (15 mL) and cooled to 0-5 C. To this cooled solution, 40 % aq. monomethyl amine solution (5.0 mL) was added and stirred at ca. 29 C over a period of 1 h. The reaction mixture was diluted with water (100 mL) and extracted with dichloromethane. The organic layer was separated, dried over anhydrous Na2SO4 and evaporated under reduced pressure to afford yellow oil.
The oil was purified through column chromatography to afford 4-Chloro-N-{[8-chloro-l-(2, 4-dichloro-phenyl)-1, 4, 5, 6-tetrahydro-1, 2-diaza-benzo [e] azulene-3-yl]-methylamino-methylene}-benzene sulfonamide (0.175 g, 0.294 mmol) as title compound 1, a white solid.

'HNMR: (CDC13, 300 MHz) 4 7.8 (d, J= 7.5 Hz, 2H), 7.4 (d, J= 7.5 Hz, 2H), 7.39 (d, J=
8.4 Hz, 1H), 7.34 (d, J= 1.8 Hz, 1H), 7.3 (m, 2H), 7.0 (d, J= 8.4 Hz, 1H), 6.5 (d, J= 5.4 Hz, 1H), 3.27 (d, J= 5.1 Hz, 2H), 3.18 (d, J= 5.1 Hz, 1H), 2.6 (m, 3H), 1.5 (s, 3H).
Example 2 Hydrochloride salt of 8-chloro-l- (2, 4-dichloro-phen )-4, 5-dihydro-1H-6-oxa-1, 2-diaza-benzo [e] azulene-3-carboxylic acid piperidin-1-ylamide.
a) 8-Chloro-l-(2, 4-dichloro-phenyl)-4, 5-dihydro-lH-6-oxa 1, 2-diaza .- benzo [e]
azulene-3-carboxylic acid by suitable modifications of similar techniques and processes known in the art.
b) Hydrochloride salt of 8-Chloro-l- (2, 4-dichloro-phenyl)-4, 5-dihydro-1H-6-oxa 1, 2-diaza - benzo [e] azulene-3-carboxylic acid piperidin- 1- yl- amide (Compound 2).
8-chloro-l- (2, 4-dichloro-phenyl)-4, 5-dihydro-1H-6-oxa 1, 2-diaza - benzo [e]
azulene-3-carboxylic acid (0.500 g, 1.221 mmol) was coupled with 1-amino-piperidine (0.197 mL, 1.832 mmol) in presence of 1-Hydroxy-benzotriazole monohydrate (HOBt.
H20), 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC-HCl) and TEA in dichloromethane (25 mL) at ca. 27 C over a period of 25-30 min. The reaction was diluted with H2O (30 mL) and extracted with dichloromethane. The dichloromethane layer was separated, dried over anhydrous Na2SO4 and evaporated under reduced pressure to afford brown oil. The brown oil was taken in anhydrous methanol and treated with ethereal HCl (ca. 4 mL) at 0-5 T. Solvents were removed under reduced pressure and residue was triturated in ethyl acetate to afford solid. The solid was filtered, washed with diethyl ether to afford title compound 2 (0.43 5 g, 0.824 mmol) as light brown solid. 'HNMR: (CDC13, 300 MHz) S 9. 35 (s, 1H), 7.51 (d, J=
1.74 Hz, 1H), 7.40 (m, 2H), 7.34 (m, 1H),.7. 14 (d, J= 1.95 Hz, 1H), 6.62 (d, J= 8.55 Hz, 1H), 4.38 (m, 2H), 4.06 (bs, 3H), 3.48. (bs, 3H), 3.26 (m, 2H), 3.11 (m, 2H), 1.67(bs, 4H), 1.41(m, 1H), 1.18 (m, 1H).

(DMSO-D6, 300 MHz) S 10.53 (s, 1H), 7.89 (d, J= 2.01 Hz, 1H), 7.78 (d, J= 8.49 Hz, '1H), 7.68 (dd, J= 10.47, 1.95 Hz, 1H), 7.26 (d, J= 1.95 Hz, 1H), 7.03 (dd, J=

10.56, 1.95 Hz, 1H), 6.72 (d, J= 8.61 Hz, 1H), 4.45 (bs, 1H), 4.25 (bs, 1H), 3.23 (bs, 4H), 3.06 (m, 3H), 1.72 (bs, 4H), 1.42(bs, 2H), 1.16(t, 1H), 0.98 (t, 1H).

Following compounds were prepared by' suitable modifications, variations of reactants, reaction conditions, reaction steps of the processes described for the synthesis of compound 2.

Compound 3:
Hydrochloride salt of 8-chloro-l-(2, 4-dichloro-phenyl)-4, 5-dihydro-lH-6-oxa-1, 2-diaza-benzo [e] azulene-3-carboxylic acid -(4-hydroxy-piperidin-1-yl -amide.
'HNMR: (CDC13, 300 MHz) 6 10.26 (bs, 1H), 7.9 (d, J= 2.1 Hz, 1H), 7.7 (d, J=
8.4 Hz, 1H), 7.6 (dd, J= 1.8 Hz, 1H), 7.2 (d, J= 1.8 Hz, 1H), 7.0 (dd, J= 6.8, 2.1 Hz, 1H), 3.38 (bs, 2H), 3.21 (bs, 4H), 3.0(bs, 4H), 2.7 (bs, 2H).
Compound 4:
Hydrochloride salt of 8-chloro-l-(2, 4-dichloro-phenyl)-4, 5-dihydro-lH-6-oxa-1, 2-diaza-benzo [e] azulene-3-carboxylic acid pyrrolidin-1-yl amide.

'HNMR: (CDC13, 300 MHz) 6 8.70 (dd, J= 6.66 Hz, 1H), 7.90 (m, 1H), 7.71 (dd, J=
6.33, 2.19 Hz, 1H), 7.26 (d, J= 2.10 Hz, 1H), 7.03 (dd, J= 6.45, 2.16 Hz, 1H), 6.72 (d, J= 8.55 Hz, 1H), 4.47 (m, 1H), 4.25 (m, 2H), 1.90-1.80(bs, 6H), 1.79 (m, 1H), 1.23-1.15 (m, 1H).
Compound 5:
Hydrochloride salt of 8-chloro-l-(2, 4-dichloro-phenyl)-4, 5-dihydro-lH-6-oxa-1, 2-diaza-benzo [e] azulene-3-carboxylic acid (hexahydro-cyclopenta[c] pyrrol-2-yl)-amide.

'HNMR: (CDC13, 300 MHz) 6 9.24 (s, 1H), 7.60 (s, 1H); 7.51 (m, 2H), 7.15 (d, J= 1.86 Hz, 2H), 6.82 (m, 1H), 6.62 (d, J= 8.49 Hz, 1H), 4.45 (bs, 2H), 3.96 (bs, 3H), 3.71 (bs, 211), 3.38 (bs, 2H), 3.27 (bs, 2H), 1.73(bs, 6H).

(DMSO-D6) 6 11.03 (s, 1H), 7.90 (d, J= 1.86 Hz, 111), 7.79 (d, J= 8.52 Hz, 111), 7.70 (dd, J= 10.41, 1.89 Hz, 1H), 7.26 (d, J= 1.83 Hz, 1H), 7.04 (dd, J= 10.41, 1.83 Hz, 1H), 6.73 (d, J= 8.58 Hz, 1H), 4.50 (bs, 1H), 4.25 (bs, 2H), 3.69 (bs, 2H), 3.45 (m, 11-1), 3.40 (m, 1H), 3.06 (bs, 2H), 2.96 (bs, 2H), 1.71 (bs, 4H), 1.62 (bs, 2H).
Compound 6:
Hydrochloride salt of 8-chloro-l-(2, 4-dichloro-phenyl)-4, 5-dihydro-lH-6-oxa-1, 2-diaza-benzo [e] azulene-3-carboxylic acid morpholine-4-yl-amide.

'HNMR: (DMSO-D6, 300 MHz) S 9.4 (s, 1H), 7.8 (d, J= 2.1 Hz, 1H), 7.7 (d, J=
8.7 Hz, I H), 7.6 (dd, J= 6.3, 2.1 Hz, I H), 7.2 (d, J= 2.1 Hz, 1H), 7.0 (dd, J= 6.4, 2.1 Hz, I H), 6.7 (d, J= 8.4 Hz, I H), 4.4 (m, 1H), 4.2 (m, 1H), 3.6 (m, 4H), 2.8 (m, 4H), 1.22 (s, 2H).
Compound 7:
Hydrochloride salt of 8-chloro-l-(2, 4-dichloro-phenyl)-4, 5-dihydro-lH-6-oxa-1, 2-diaza-benzo [e] azulene-3-carboxylic acid (4-methyl-piperazine-1-yl)-amide.
'HNMR: (DMSO-D6, 300 MHz) S 9.7 (s, 1H), 7.8 (d, J= 2.1 Hz, 1H), 7.7 (d, J=
8.7 Hz, 1H), 7.6 (dd, J= 6.3, 2.1 Hz, 1H), 7.2 (d, J= 2.4 Hz, 1H), 7.0 (dd, J= 6.4, 2.1 Hz, 1H), 6.7 (d, J= 8.4 Hz, 1H), 4.4 (m, 1H), 4.2 (m, 1H), 3.7 (m, 1H), 3.1 (bs, 4H), 2.7 (s, 3H), 1.22 (s, 4H).
Compound 8:

Hydrochloride salt of 8-chloro-l-(4-chloro-phenyl)-4, 5-dihydro-1H-6-oxa-1, 2-diaza-benzo [e] azulene-3-carboxylic acid piperidin-1-ylamide.

'HNMR: (DMSO-D6, 300 MHz) S 11.0 (s, 1H), 7.58 (d, J= 8.4 Hz, 2H), 7.4 (d, J=
8.7 Hz, 2H), 7.2 (d J= 2.1 Hz, 1H), 7.0 (dd, J= 6.6, 1.8 Hz, 1H), 6.7 (d, J= 8.4 Hz, 1H), 4.3 (t, J= 6.6 Hz, 2H), 3.1 (bs, 4H), 2.7 (d, J- 4.8 Hz, 2H), 1.97 (bs, 4H), 1.4 (bs, 2H).
Compound 9:
Hydrochloride salt of 8-chloro-l-(4-chloro-phenyl)-4, 5-dihydro-lH-6-oxa-1, 2-diaza-benzo [e] azulene-3-carboxylic acid pyrrolidin-1-ylamide.
'HNMR: (DMSO-D6,300 MHz) S 9.1 (s, 1H), 7.5 (d, J= 8.7 Hz, 2H), 7.4 (d, J= 8.7 Hz, 2H), 7.2 (d, J= 2.1 Hz, 1H), 7.0 (dd, J= 6.3, 2.1 Hz, I H), 6.7 (d, J= 8.4 Hz, I H), 4.3 (t, J= 6.3 Hz, 2H), 3.1 (bs, 4H), 2.7 (d, J= 4.8 Hz, 2H), 1.97 (bs, 4H), 1.4 (bs, 2H).
Compound 10:
Hydrochloride salt of 8-chloro-l-(4-chloro-phenyl)-4, 5-dihydro-1H-6-oxa-1, 2-diaza-benzo [e] azulene-3-carboxylic acid morpholin-4-ylamide.
'HNMR: (DMSO-D6,300 MHz) 6 9.5 (s, 1H), 7.5 (d, J= 8.4 Hz, 2H), 7.4 (d, J= 8.7 Hz, 2H), 7.2 (d, J= 2.1 Hz, 1H), 7.0 (dd, J= 6.6, 2.1 Hz, 1H), 6.7 (d, J= 8.7 Hz, 1H), 4.3 (t, J= 6.6 Hz, 2H), 3.2 (t, J= 6.6 Hz, 2H), 3.0 (m, 2H), 2.8(m, 4H), 2.7 (m, 2H).
Compound 11:
Hydrochloride salt of 8-chloro-l-(4-chloro-phenyl)-4, 5-dihydro-1H-6-oxa-1, 2-diaza-benzo [e] azulene-3-carboxylic acid -N'-cyclopropyl-hydrazide.

'HNMR: (DMSO-D6, 300 MHz) S 10.7 (s, 1H), 8.3 (d, J= 4.5 Hz, 1H), 7.7 (d, J=
8.4 Hz, 1H), 7.6 (dd, J= 6.3, 2.1 Hz, 1H), 7.2 (d, J=2.1 Hz, 1H), 7.0 (dd, J= 6.6, 2.1 Hz, 1H), 6.7 (d, J= 8.7 Hz, 1H), 4.4 (m, 4H), 4.0 (m, 4H), 2.8 (m, 2H), 0.5(m, 5H).

Compound 12:
Hydrochloride salt of 8-chloro-l-(4-chloro-phenyl)-4, 5-dihydro-lH-6-oxa-1, 2-diaza-benzo [e] azulene-3-carboxylic acid piperidin-1-ylamide.
'HNMR: (DMSO-D6, 300 MHz) S 10.66 (s, 1H), 7.52 (s, 3H), 7.39 (d, J= 2.9 Hz, 2H), 7.27 (s, 1H), 6.99 (d, J= 8.55 Hz, 1H), 4.40 (t, J= 5.95 Hz, 2H), 3.56 (t, J=
6.0 Hz, 3H), 3.18 (d, J= 6.99 Hz, 4H), 1.74 (s, 3H), 1.43(s, 2H).
Compound 13:
Hydrochloride salt of 1-(2, 4-Dichloro-phenyl)-8-methyl-4, 5-dihydro-1H-6-oxa-1, 2-diaza-benzo [e] azulene-3-carboxylic acid piperidin-1-yl amide.

'HNMR: (CDC13, 300 MHz) S 9.53 (s, 1H), 7.50 (s, 1H), 7.39(m, 2H), 6.91 (s, 1H), 6.64 (d, J= 7.66 Hz, 1H), 6.56 (d, J= 8.09 Hz, 1H), 4.13 (bs, 4H), 4.05 (bs, 4H), 3.48 (bs, 3H), 2.28 (s, 3H), 2.06 (s, 4H).
Compound 14:
Hydrochloride salt of 1-(2, 4-Dichloro-phenyl)-8-methyl-4, 5-dihydro-1H-6-oxa-1, 2-diaza-benzo [e] azulene-3-carboxylic acid pyrrolidin-1-ylamide.
'HNMR: (CDC13, 300 MHz) S 9.31(s, 1H), 7.51(s, 1H), 7.40(m, 2H), 6.91 (s, 1H), 6.58 (m, 2H), 4.36 (bs, 2H), 3.90 (bs, 4H), 3.39 (bs, 2H), 2.28 (bs, 6H).
(DMSO-D6) 11.70 (s, 1H), 7.99 (d, J= 2.13 Hz, 1H), 7.75 (d, J- 8.49 Hz, 1H), 7.68 (dd, J= 8.52, 2.16 Hz, 1H), 6.95 (s, 1H), 6.71 (d, J= 7.35 Hz, 1H), 6.59 (d, J=
8.07 Hz, 1H), 4.4 (m, 1H), 4.21(m, 1H), 3.56 (bs, 1H), 3.34 (m, 2H), 2.21 (s, 3H), 1.21 (bs, 4H).
Compound 15:
Hydrochloride salt of 1- (4-chloro-phenyl)-8-methyl-4, 5-dihydro-1H-6-oxa-1, 2-diaza-benzo [e] azulene-3-carboxylic acid piperidin-1-ylamide.
'HNMR: (DMSO-D6, 300 MHz) S 11.15 (s, 1H), 7.58 (d, J= 8.52 Hz, 1H), 7.40 (d, J=
8.52 Hz, 2H), 6.99 (s, 1H), 6.75 (d, J=7.95 Hz, 1H), 6.63 (d, J= 8.01 Hz, 1H), 4.30 (bs, 2H), 3.75 (t, 2H), 3.37 (s, 4H), 3.24 (t, 2H), 2.24 (s, 3H), 1.80 (s, 4H), 1.46 (m, 2H).
Compound 16:
Hydrochloride salt of 1-([8-chloro-l- (2, 4-dichloro-phenyl)-1, 4, 5, 6 -tetrahydro-7-thia-1, 2-diaza-cyclopenta [e] azulene-3-carboxylic acid piperidin-l-ylamide.

1HNMR: (CDC13, 300 MHz) S 9.4 (s, 1H), 7.60 (s, 1H), 7.4 (d, 2H), 5.9 (s, 1H), 3.9 (bs, 5H), 3.1 (s, 3H), 2.9 (t, 2H), 2.1 (bs, 6H).
Compound 17:
Hydrochloride salt of 8-Chloro-l-(2, 4-dichloro-phenyl)-1, 4, 5, 6-tetrahydro-thia-1, 2-diaza-cyclopenta [e] azulene-3-carboxylic acid (hexahydro-cyclopenta [c]
pyrrol-2-yl)-amide.

1HNMR: (CDC13, 300 MHz) S 9.4 (s, 1H), 7.50 (s, 1H), 7.4 (d, 2H), 5.9 (s, 1H), 4.4 (bs, 2H), 3.9 (bs, 2H), 3.1 (s, 2H), 3.0 (bs, 2H), 2.8 (t, 2H), 2.0 (bs, 2H), 1.9-1.6 (m, 6H).
Compound 18:
Hydrochloride salt of 8-Chloro-l-(2, 4-dichloro-phenyl)-4, 5-dihydro-1H-6, 7-dithia-1', 2-diaza-cyclopenta [e] azulene-3-carboxylic acid piperidin-1-ylamide. .
1HNMR: (CDC13,300 MHz) S 9.4 (s, 1H), 7.50 (s, 1H), 7.4 (d, 3H), 6.1 (s, 1H), 3.9 (bs, 4H), 3.4 (d, J= 5.8 Hz, 2H), 3.2 (d, J= 5.46 Hz, 2H), 2.1 (s, 6H).
Compound 19:
Hydrochloride salt of 7-Chloro-l-(2, 4-dichloro-phenyl)-1, 5-dihydro-4, 6-dithia- 1, 2-diaza-as-indacene-3 -carboxylic acid piperidin-l-ylamide.

1HNMR: (DMSO-D6, 300 MHz) S 10.62 (bs, 1H), 8.10 (s, 1H), 7.85 (d, J= 8.49 HZ, 1H), 7.71 (dd, J= 8.49, 2.1 Hz, 1H), 6.08 (s, 1H), 4.23 (s, 2H), 2.89 (m, 4H), 1.67 (m, 41-1), 1.10 (m, 6H).
Compound 20:
Hydrochloride salt of 7-Chloro-l-(2, 4-dichloro-phenyl)-1, 5-dihydro-4, 6-dithia-1, 2-diaza-as-indacene-3-carboxylic acid (hexahydro-cyclopenta [c]
pyrrol-2-yl)-amide.

1HNMR: (DMSO-D6, 300 MHz) S 11 (s, 1H), 8.04 (d, J= 2.1 Hz, 1H), 7.87 (d, J=
8.5 HZ, 1H), 7.76 (dd, J= 8.5, 2.1 Hz, 111), 6.06 (s, 1H), 4.2 (s, 3H), 3.6 (bs, 2H), 2.9 (s, 2H), 2.8 (d, 2H), 1.9 (bs, 2H).
Compound 21:
Hydrochloride salt of 8-Chloro-l-(2, 4-dichloro-phenyl)-4, 5-dihydro-lH-6-thia-1, 2-diaza-benzo [e] azulene-3-carboxylic acid piperidin-l-ylamide 1HNMR: (DMSO-D6, 300 MHz) S 10.55 (s, 1H), 7.88 (d, J= 2.01 Hz, 1H), 7.80 (d, J=
8.50 Hz, 1H), 7.70 (dd, J= 10.46, 1.93 Hz, 1H), 7.24 (d, J= 1.92 Hz, 1H), 7.05 (dd, J=
10.56, 1.93 Hz, 1H), 6.75 (d, J= 8.63 Hz, 1H), 4.47 (bs, 1H), 4.23 (bs, 1H), 3.25 (bs, 4H), 3.04 (m, 3H), 1.75 (bs, 4H), 1.40(bs, 2H), 1.18(t, 1H), 1.00(t, 1H).

Compound 22:
Hydrochloride salt of 8-Bromo-l-(2, 4-dichloro-phenyl)-4, 5-dihydro-1H-6-oxa-1, 2-diaza-benzo [e] azulene-3-carboxylic acid piperidin-1-ylamide.
'HNMR: (DMSO-D6, 300 MHz) S 10.52 (s, 1H), 7.86 (d, J= 2.01 Hz, 1H), 7.73 (d, J=
8.40 Hz, 1H), 7.66 (dd, J= 10.43, 1.98 Hz, IH), 7.30 (d, J= 1.99 Hz, 1H), 7.08 (dd, J=
10.44, 1.98 Hz, 1H), 6.73 (d, J= 8.50 Hz, 1H), 4.48 (bs, IH), 4.22 (bs, 1H), 3.25 (bs, 4H), 3.08 (m, 3H), 1.77 (bs, 4H), 1.42(bs, 2H), 1.18(t, 1H), 0.99 (t, 1H).
Biological activity Compounds of the present invention in the cAMP accumulation model, antagonizes the WIN-55, 212-2 inhibition of forskolin-induced cAMP
accumulation in hCBI_CHO cells [J Pharmacol. Exp: Ther., 1998, 284, 291-297]. In a mouse vas deferens preparation, representative compounds cause rightward shift of the WIN-55, 212-2 concentration-response curve (Eur. J. Pharm. 1995, 284, 241-247).
Representative compounds of the present invention have shown decrease in sucrose solution intake in rat model (Table 1) [Psychopharmacology, 1997, 132, 104-106].
Table 1: Effect of representative compounds on the intake of 5 % sucrose solution in animal model.

Compound No. Reduction in sucrose solution consumption w.r.t. control animals 3 -18.9 14.0 5 -23.2 11.4 6 -24.9 8.9 8 -30.4 4.3 16 -13.2 15.7 * formula for calculation :
[Total consumption - Mean total consumption of control]

[Mean total consumption by control]
number of animals in a group = 6.
No significant adverse effects were observed for any of the mentioned compounds of invention.

Claims (15)

1. Compounds of general formula (I):

their tautomeric forms, their pharmaceutically acceptable salts, wherein `Ar' represents single or fused groups selected from aryl, optionally substituted with groups selected from halo, optionally substituted linear alkyl, and optionally substituted branched alkyl groups;
`A' represents a substituted aryl and X is selected from O, S, SO, SO2 and NR', where R' represents H, or an optionally substituted group selected from linear alkyl, branched alkyl, and cycloalkyl groups, and m & n each represent an integer such that m is 1 or 2 and n is 1, 2 or 3; and wherein the substitution on A is selected from halogen, hydroxyl, and substituted groups selected from linear and branched alkyl groups;
R1 represents O or S; R2 is either H or C1-C6 alkyl; R3 is -NR b R c, where R
b & R c each represents an optionally substituted group selected from alkyl, aralkyl and alkenyl, or R b & R c together with the nitrogen atom to which they are bonded, form a saturated or unsaturated heterocyclic or heteroaromatic radical.

2. The compound as claimed in claim 1, wherein the alkyl of X and/or R3 is a linear or branched alkyl group comprising from one to eight carbon atoms.

3. The compound as claimed in claim 1, wherein the aryl of A and/or Ar is selected from monocyclic, bicyclic and tricyclic aryl groups.

4. The compound as claimed in any one of claims 1 to 3 wherein the aryl of A
and/or Ar is selected from phenyl, naphthyl, tetrahydronaphthyl, indane, and biphenyl groups.

5. The compound as claimed in claim 1 wherein the heterocyclyl of R b and R c is selected from saturated, partially saturated, unsaturated aromatic and non-aromatic mono, bi and tricyclic groups, containing one or more heteroatoms selected from N, O, and S.

6. The compound as claimed in any one of claims 1 to 5 wherein the heterocyclyl of R b and R c is selected from aziridinyl, azetidinyl, pyrrolidinyl, imidazolidinyl, piperidinyl, piperazinyl, 2-oxopiperidinyl, 4-oxopiperidinyl, 2-oxopiperazinyl, 3 -oxopiperazinyl, morpholinyl, thiomorpholinyl, 2-oxomorpholinyl, azepinyl, diazepinyl, oxapinyl, thiazepinyl, oxazolidinyl, thiazolidinyl, dihydrothiophene, dihydropyran, dihydrofuran, dihydrothiazole, benzopyranyl, benzopyranonyl, benzodihydrofuranyl, benzodihydrothienyl, pyrazolopyrimidonyl, azaquinazolinoyl, thienopyrimidonyl, quinazolonyl, pyrimidonyl, benzoxazinyl, benzoxazinonyl, benzothiazinyl, benzothiazinonyl, and thieno piperidinyl groups.

7. The compound as claimed in claim 1 wherein the heteroaryl of R b and R c is selected from optionally fused mono, bi and tricyclic heteroaromatic groups comprising one or more hetero atoms selected from O, N and S.

8. The compound as claimed in any one of claims 1 to 7 wherein the heteroaryl of R b and R c is selected from pyridyl, thienyl, furyl, pyrrolyl, oxazolyl, thiazolyl, isothiazolyl, imidazolyl, isoxazolyl, oxadiazolyl, thiadiazolyl, triazolyl, tetrazolyl, benzofuranyl, benzothienyl, indolinyl, indolyl, azaindolyl, azaindolinyl, pyrazolopyrimidinyl, azaquinazolinyl, pyridofuranyl, pyridothienyl, thienopyrimidyl, quinolinyl, pyrimidinyl, pyrazolyl, quinazolinyl, pyridazinyl, triazinyl, benzimidazolyl, benzotriazolyl, phthalazynil, naphthylidinyl, purinyl, carbazolyl, phenothiazinyl, phenoxazinyl, benzoxazolyl, and benzothiazolyl groups.

9. The compound as claimed in any one of claims 1 to 8 selected from:
8-chloro-l-(2, 4-dichloro-phenyl)-4, 5-dihydro-1H-6-oxa-1, 2-diaza-benzo [e]
azulene-3-carboxylic acid piperidin-1-ylamide and its pharmaceutically acceptable salts;

8-chloro-1-(2, 4-dichloro-phenyl)-4, 5-dihydro-1H-6-oxa-1, 2-diaza-benzo [e]
azulene-3-carboxylic acid pyrrolidin-1-yl amide and its pharmaceutically acceptable salts;
8-chloro- 1 -(2, 4-dichloro-phenyl)-4, 5-dihydro-1H-6-oxa- 1,2-diaza-benzo [e]

azulene-3-carboxylic acid (hexahydro-cyclopenta[c] pyrrol-2-yl)-amide and its pharmaceutically acceptable salts;
8-chloro-1-(2,4-dichloro-phenyl)-4, 5-dihydro-1H-6-oxa-1,2-diaza-benzo [e]
azulene-3-carboxylic acid morpholine-4-yl-amide and its pharmaceutically acceptable salts;
8-chloro- 1 -(4-chloro-phenyl)-4, 5-dihydro-1H-6-oxa-1, 2-diaza-benzo [e]
azulene-3-carboxylic acid piperidin-1-ylamide and its pharmaceutically acceptable salts;

8-chloro-1-(4-chloro-phenyl)-4, 5-dihydro-1H-6-oxa-1, 2-diaza-benzo [e]
azulene-3-carboxylic acid pyrrolidin-1-ylamide and its pharmaceutically acceptable salts;
8-chloro-1-(4-chloro-phenyl)-4, 5-dihydro-1H-6-oxa-1, 2-diaza-benzo [e]
azulene-3-carboxylic acid morpholin-4-ylamide and its pharmaceutically acceptable salts;

8-chloro-1-(4-chloro-phenyl)-4, 5-dihydro-1H-6-oxa-1, 2-diaza-benzo [e]
azulene-3-carboxylic acid N'-cyclopropyl-hydrazide and its pharmaceutically acceptable salts;
1-(2, 4-Dichloro-phenyl)-8-methyl-4, 5-dihydro-1H-6-oxa-1,2-diaza-benzo [e]
azulene-3-carboxylic acid piperidin-1-ylamide and its pharmaceutically acceptable salts;
1-(2, 4-Dichloro-phenyl)-8-methyl-4, 5-dihydro-1H-6-oxa- 1,2-diaza-benzo [e]
azulene-3-carboxylic acid pyrrolidin-1-ylamide and its pharmaceutically acceptable salts;

1-(4-chloro-phenyl)-8-methyl-4, 5-dihydro-1H-6-oxa-1,2-diaza-benzo [e] azulene-carboxylic acid piperidin-1-ylamide and its pharmaceutically acceptable salts;

8-chloro-1-(2, 4-dichloro-phenyl)-4,5-dihydro-1H-6-thia-1,2-diaza-benzo [e]
azulene-3-carboxylic acid piperidin-1-ylamide and its pharmaceutically acceptable salts; and 8-Bromo-1-(2, 4-dichloro-phenyl)-4, 5-dihydro-1H-6-oxa- 1,2-diaza-benzo [e]
azulene-3-carboxylic acid piperidin-1-ylamide and its pharmaceutically acceptable salts.

10. A pharmaceutical composition which comprises a compound of formula (I), as claimed in any one of claims 1 to 9 and a pharmaceutically acceptable carrier, diluent or excipient.

11. A medicine for treatment and/or reduction of a disease associated with cannabinoid receptors, the medicine comprising a compound of formula (I) as claimed in any one of claims 1 to 9, or a pharmaceutically acceptable salt thereof or a pharmaceutically acceptable composition containing the compound or salt thereof.

12. Use of a compound of formula (I) as claimed in any one of claims 1 to 9, or a pharmaceutically acceptable salt thereof, or a pharmaceutical composition or medicine containing the compound or salt thereof, as a medicament suitable for the treatment of diseases associated with the cannabinoid system.

13. A process of preparing a compound of formula (I) according to any one of claims 1 to 9, comprising the steps of:
i) converting a compound of formula (2) to a compound of formula (4) by reacting with a suitable substituted hydrazine hydrochloride of formula (3), in a suitable solvent where A, Ar are as defined in claim 1 and R represents an alkyl group selected from a linear or branched radical containing one to eight carbons ii) hydrolyzing the compound of formula (4) with a suitable hydrolyzing agent in a suitable solvent to obtain a compound of formula (5), where A, Ar, X are as defined in claim 1 either iii) converting the compound of formula (5) to a compound of formula (I) by treating with a suitable halogenating agent and a suitable substituted amine of formula NHR 2 R 3 in a suitable solvent, where A, Ar, X, R2 & R3 are as defined in claim 1, or iv) alternatively, converting the compound of formula (5) to a compound of formula (7) by treatment with a compound of formula NH 2 Q, in suitable solvent where A, Ar, X is as defined in claim 1 and Q represents H, a substituted or unsubstituted group selected from alkyl, aralkyl, aryl, heteroaryl or heterocyclic group or a group represented by SO 2 R" where R" represents H, -OH, halogen or substituted or unsubstituted groups selected from alkyl, aralkyl, aryl, heteroaryl, heterocyclic and alicyclic groups v) converting the compound of formula (7) to a compound of formula (8) by reacting with a suitable halogenating agent in suitable solvent, where A, Ar and X
are as defined in claim 1 and Q is as defined as above and vi) converting the compound of formula (8) to a compound of formula (I) by treatment with a suitable substituted amine of formula NHR 2 R 3 in a suitable solvent where A, Ar, X, R2 and R3 are as defined in claim 1

14. A process as claimed in claim 13, wherein in step (i), the suitable solvent is selected from MeOH, EtOH, propanol, isopropanol, butanol, t-butanol, and acetic acid and mixtures thereof;
in step (ii), the suitable hydrolyzing agent is selected from NaOH, KOH, LiOH, AgNO 3, Na 2 CO 3, and CsCO 3 and the suitable solvents are selected from methanol, methanol/water, methanol/THF and THF/H 2 O;
in step (iii), the suitable halogenating agent is selected from SOCl 2, COCl 2, PCl 3, and PCl 5 and the suitable solvent is selected from toluene, benzene, xylene, dichloromethane, and chloroform and mixtures thereof;
in step (iv), the suitable solvent is selected from triethyl amine, DMSO, DMF, and diisopropyl ethyl amine;
in step (v), the suitable halogenating agent is selected from SOCl 2, COCl 2, PCl 3, and PCl 5 and the suitable solvent is selected from toluene, benzene, xylene, dichloromethane and chloroform; and in step (vi), the suitable solvent is selected from methanol, ethanol, water and THF.

15. An intermediate compound of the formula:
wherein `A' represents substituted aryl, X is selected from O, S, SO, SO2, and NR', where R' represents H, or an optionally substituted group selected from a linear or branched alkyl, and cycloalkyl groups and m & n represents integers such that m is 1 or 2 and n is 1, 2 or 3; the substitution on A is selected from halogen, hydroxyl, and substituted groups selected from linear and branched alkyl groups; and R
represents an alkyl group which is a linear or branched radical containing one to eight carbons.